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Acute Salt Handling in Orthostatic Intolerance

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Vanderbilt University

Status

Active, not recruiting

Conditions

Orthostatic Tachycardia
Orthostatic Intolerance
Postural Tachycardia Syndrome

Treatments

Other: normal saline (0.9%)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00581633
K23RR020783 (U.S. NIH Grant/Contract)
061230
UL1RR024975 (U.S. NIH Grant/Contract)
P01HL056693 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The investigators will test the hypothesis that patients with chronic orthostatic intolerance or postural orthostatic tachycardia syndrome (OI or POTS) will be unable to conserve urinary sodium as compared to healthy control subjects.

Full description

Patients with chronic OI appear to be hypovolemic with abnormalities in hormones that regulate salt & water handling. Increases in dietary salt have salutary effects on orthostatic tolerance in a physiological laboratory. The infusion of intravenous saline acutely decreased heart rate in this patient population. Preliminary data from Vanderbilt suggests abnormal salt handling in patients with chronic OI in a few patients. These data need to be confirmed and a better understanding of sodium handling in response to acute salt loads is required in these patients.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diagnosed with orthostatic intolerance by Vanderbilt Autonomic Dysfunction Center (or healthy control subject)

Exclusion criteria

  • Overt or acute cause for orthostatic tachycardia
  • Hypertension (BP>145/95 or need for anti-hypertensive medications)
  • QRS duration > 120 msec on EKG
  • Pregnancy

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

1
Experimental group
Description:
saline infusion for sodium loading
Treatment:
Other: normal saline (0.9%)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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